NAKED SUNDAYS BEACH DAY ALL OVER WATER MIST SPF 45- broad spectrum spf45 liquid

NAKED SUNDAYS BEACH DAY ALL OVER WATER MIST by

Drug Labeling and Warnings

NAKED SUNDAYS BEACH DAY ALL OVER WATER MIST by is a Otc medication manufactured, distributed, or labeled by WILD CHILD LABORATORIES PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Active Ingredients:

Avobenzone 1.5%

Octocrylene 5%

Phenylbenzimidazole Sulfonic Acid 3%

Purpose

Sunscreen

USES

Uses: Helps prevent sunburn. If used as
directed with other sun protection measures
(see directions), decreases the risk of skin
cancer and early skin ageing caused by the sun.

WARNINGS

Warnings: For external use only. Do not use
on damaged or broken skin

Keep out of eyes, Rinse with water to remove

Keep out of reach of children.
Stop use and ask a doctor if rashes occur.
If product is swallowed, get medical help or
contact a Poison Control Center right away.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• SPRAY 7 TIMES WITH MOUTH AND LIPS CLOSED 8-10" AWAY FROM FACE 15 MINUTES BEFORE SUN EXPOSURE.
• Reapply after 80 minutes of swimming or sweating.
• Reapply immediately after towel drying.
• Reapply at least every 2 hours.
• Children under 3 years of age: Ask a doctor.

SUN PROTECTION MEASURES:

Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

• Limit time in the sun, especially from 10.00AM - 2.00PM
• Wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENTS

Purified water, Sorbitol. Pentylene glycol , Hydroxyapatite, PEG/PPG Dimethicone, Potassium Chloride, Phenoxyethanol, Citrullus lantus , Sodium Hydroxide, Hydroxyacetophenone, Microcrystalline Cellulose, Cellulose gum, Silica, Ethylhexylglycerin, PVP, Fragrance ( Natural) , Aloe Barbadensis Leaf Juice, Sodium Benzoate

OTHER INFORMATION

Other Information: Protect this product
from excess heat and direct sun. Store below
30°C / 86°F.

USER SAFETY WARNINGS

Directions: Avoid Eye Area, Shake well before use.

Use as top up sunscreen only. Hold 8-10" away from your body and spray liberally & evenly until skin feels moist 15 minutes before sun exposure. Do not spray directly on to face. Make sure no spots are missed by spraying onto hands and applying to face. DO not apply in windy conditions.

Use in well-ventilated area. Avoid inhalation. Use a water resistant sunscreen if swimming or sweating. Reapply immediately after towel drying. Reapply at least every 2 hours.

Children under 6 months of age ask a doctor

PURPOSE

Sunscreen

ASK DOCTOR

If rashes occur

OTHER SAFETY INFORMATION

Sun Protection measure

Spending time in the sun increases your risk of skin cancer and early skin aging,To decrease this risk regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measure including: Limit time in the sun,especially from 10:00 AM to 02:00 PM. Wea long sleeved shirts pants hats and sunglasses

Label

INGREDIENTS AND APPEARANCE

NAKED SUNDAYS BEACH DAY ALL OVER WATER MIST  SPF 45
broad spectrum spf45 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30807-2510
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 mL
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	3 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
PEG-9 DIMETHICONE (UNII: 9OZ27X065D)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POVIDONE (UNII: FZ989GH94E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30807-2510-1	70 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/18/2024

Labeler - WILD CHILD LABORATORIES PTY LTD (890661643)